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Clinical Trial Summary

The primary objective of this study is to assess the safety and efficacy of voclosporin as therapy in subjects with active noninfectious uveitis involving the intermediate and/or posterior segments of the eye (i.e., anterior + intermediate-, intermediate-, posterior- or pan-uveitis).


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01243983
Study type Interventional
Source Lux Biosciences, Inc.
Contact
Status Completed
Phase Phase 3
Start date February 2011
Completion date December 2012

See also
  Status Clinical Trial Phase
Terminated NCT03207815 - Study to Evaluate the Efficacy and Safety of Filgotinib in Adults With Active Noninfectious Uveitis Phase 2
Completed NCT01789320 - Safety Study of Suprachoroidal Triamcinolone Acetonide Via Microneedle to Treat Uveitis Phase 1/Phase 2